Variant #0000566702 (NC_000019.9:g.1912062del, NM_138422.2:c.16del (ADAT3))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1912062del
DNA change (hg38) g.1912063del
Published as ADAT3(NM_138422.4):c.16delC (p.R6Vfs*10)
ISCN -
DB-ID ADAT3_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCAMP4 NM_079834.2 ?/. - c.-41-2916del r.(=) p.(=)
ADAT3 NM_138422.2 ?/. - c.16del r.(?) p.(Arg6ValfsTer10)


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